Coordination chemistry of alkali metals in a modified β-diketiminate ligand scaffold

被引:0
作者
Burnett, Stuart [1 ]
Kennedy, Alan R. [1 ]
Weetman, Catherine E. [1 ]
机构
[1] Univ Strathclyde, Dept Pure & Appl Chem, 295 Cathedral St, Glasgow City G1 1XL, Scotland
基金
英国工程与自然科学研究理事会;
关键词
Alkali metals; Coordination chemistry; Ligand design; C-H; COMPLEXES; REACTIVITY; REDUCTION; CLEAVAGE;
D O I
10.1016/j.poly.2025.117461
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
beta-diketiminate (or NacNac) ligands are a widely used ligand class in the stabilisation of metal complexes across the periodic table, in part due to the ease of variability of the ligand steric and electronic effects either at the beta-carbon atom or the N-Ar group. Functionalisation of the gamma-carbon position is not typically observed however and examples of such complexes are scarce in the literature. Herein, we report on the synthesis and characterisation of alkali metal NacNac complexes which contain such gamma-carbon functionalisation in the form of a methyl group. Deprotonation of the beta-diketimine proligand Me3DipNacNacH 1 (Me3DipNacNacH = (CH3)C(C(CH3) NDip)2H, Dip = 2,6-iPr2-C6H3) by various alkali metal bases yielded the corresponding alkali metal complexes Me3DipNacNacAM (where AM = Li 2, Na 3, K 4, Rb 5, Cs 6) which have been fully characterised by 1H and 13C {1H} NMR spectroscopy, while 3 and 4 have been structurally characterised by single-crystal X-ray diffraction. The solid-state structures obtained illustrate the varied range of coordination modes accessible to such group 1 metal complexes.
引用
收藏
页数:6
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